Morphine Sulfate 71335-0736
Product NDC
71335-0736- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 11, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA078761
Active Ingredients
| Ingredient | Strength |
|---|---|
| Morphine Sulfate | 15 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(10)
26 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-0)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-1)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-2)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-3)
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-4)
40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-5)
14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-6)
15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-7)
20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-8)
84 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-9)